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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Carbonic anhydrase 12 | ||
| Ligand | BDBM50351136 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_764119 (CHEMBL1821330) | ||
| Ki | 9.9±n/a nM | ||
| Citation |  Brzozowski, Z; Slawinski, J; Gdaniec, M; Innocenti, A; Supuran, CT Carbonic anhydrase inhibitors. Synthesis, molecular structures, and inhibition of the human cytosolic isozymes I and II and transmembrane isozymes IX, XII (cancer-associated) and XIV with novel 3-pyridinesulfonamide derivatives. Eur J Med Chem46:4403-10 (2011) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Carbonic anhydrase 12 | |||
| Name: | Carbonic anhydrase 12 | ||
| Synonyms: | CA-XII | CA12 | CAH12_HUMAN | Carbonate dehydratase XII | Carbonic anhydrase | Carbonic anhydrase 12 (CA XII) | Carbonic anhydrase XII | Carbonic anhydrase XII (CA XII) | Carbonic anhydrase XII (CAXII) | Tumor antigen HOM-RCC-3.1.3 | ||
| Type: | Enzyme | ||
| Mol. Mass.: | 39456.00 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | Catalytic domain of human cloned isozyme was used in the assay | ||
| Residue: | 354 | ||
| Sequence: |
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| BDBM50351136 | |||
| n/a | |||
| Name | BDBM50351136 | ||
| Synonyms: | CHEMBL1817904 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C12H15N4O2S | ||
| Mol. Mass. | 279.338 | ||
| SMILES | C[N+](C)=c1ccn(cc1)-c1ccncc1S(N)(=O)=O |(26.5,-5.88,;25.16,-5.12,;25.15,-3.58,;23.83,-5.89,;23.83,-7.44,;22.5,-8.21,;21.17,-7.44,;21.16,-5.91,;22.48,-5.13,;19.84,-8.21,;18.51,-7.45,;17.18,-8.22,;17.18,-9.77,;18.51,-10.54,;19.85,-9.76,;21.18,-10.53,;21.19,-12.07,;21.94,-9.19,;22.72,-10.53,)| | ||
| Structure | 
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